[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-rd-quality-manager-senior-auditor-mwd":3,"similar-rd-quality-manager-senior-auditor-mwd":35},{"id":4,"slug":5,"title":6,"skills":7,"budget":20,"duration":20,"location":21,"onsitePercent":22,"contractType":23,"foundAt":24,"category":25,"description":29,"rawText":30,"webTitle":6,"webText":31,"language":32,"projectId":33,"sourceUrl":34},10743,"rd-quality-manager-senior-auditor-mwd","R&D Quality Manager \u002F Senior Auditor (m\u002Fw\u002Fd)",[8,9,10,11,12,13,14,15,16,17,18,19],"Audits","GCP","GxP","CAPA","Qualitätssicherung","FDA","MDR","ICH","Inspektionsmanagement","Qualitätsmanagementsysteme","Lieferantenaudits","Dokumentation",null,"Frankfurt am Main",100,"contracting","2026-06-03T08:26:45+00:00",{"id":26,"slug":27,"label":28},14,"medical_tech","Medizintechnik","Unterstützung als R&D Quality Manager \u002F Senior Auditor mit Fokus auf Planung und Durchführung von GCP-\u002FGxP-Audits, Erstellung risikobasierter Auditpläne sowie Steuerung von Qualitätsvorfällen. Beratung von Clinical Operations als QA Business Partner und Vorbereitung auf Inspektionen.","R&D Quality Manager \u002F Senior Auditor (m\u002Fw\u002Fd)\nProjektnummer: FE55-07829-WIPL\nStandort: Frankfurt am Main, Hessen\nArbeitsweise: Vor Ort\nLaufzeit: Keine Angabe\nStartdatum: Keine Angabe\n\nUnterstütze unseren Kunden als #jobtitel#:\n- Planung, Durchführung und Dokumentation von GCP-\u002FGxP-Audits (z. B. Investigator Sites, TMF, CSP\u002FCSR, CROs, Labore, Dienstleister)\n\n- Erstellung risikobasierter Auditpläne & Bewertung regulatorischer Compliance\n\n- Steuerung von Qualitätsvorfällen inkl. CAPA & Escalation Management\n\n- Weiterentwicklung des QMS (SOPs, Abweichungen, Dokumentation, Metrics)\n\n- Beratung und Unterstützung von Clinical Operations als QA Business Partner bei Qualitäts- und GCP-relevanten Fragestellungen\n\n- Durchführung und Begleitung von Lieferantenaudits sowie Unterstützung bei der Lieferantenqualifizierung\n\n- Vorbereitung und Begleitung von Inspektionen sowie Audit Readiness\n\n- Durchführung von Schulungen zu GCP, GxP und qualitätsrelevanten Prozessen\n\nDas bringst Du mit:\n- Abgeschlossenes Studium Naturwissenschaften, Pharmazie oder Medizin\n\n- Langjährige Erfahrung in der klinischen Qualitätssicherung (mind. 10 Jahre) sowie im Auditumfeld (mind. 5 Jahre)\n\n- Fundierte Kenntnisse in GCP (ICH-GCP E6), CTR, MDR sowie FDA-Regularien\n\n- Nachweisbare Erfahrung in Auditierung und Inspektionsmanagement im klinischen Umfeld\n\n- Erfahrung im Umgang mit CAPA-Prozessen und Qualitätsmanagementsystemen\n\n- Sehr gute Englischkenntnisse in Wort und Schrift\n\n- Bereitschaft zu nationalen und internationalen Dienstreisen\n\nSkills: Audits, Beratung, Bewertung, CAPA, CSP, Dokumentation, FDA, GCP, GxP, ICH, Lieferantenaudits, MDR, Management, Pharmazie, Planung, Qualitätssicherung, R&D, Steuerung\n\nAnsprechpartner:\nMelina Braun\nJunior Talent Acquisition Spezialist\nFERCHAU GmbH, Niederlassung Wiesbaden Pharma & Life Science\nAlte Schmelze 18-20\n65201 Wiesbaden\n+49 611 238 7750\nwiesbaden-pls@ferchau.com","Wir suchen einen erfahrenen R&D Quality Manager und Senior Auditor für ein etabliertes Unternehmen im Pharma- und Life-Science-Bereich am Standort Frankfurt am Main. In dieser verantwortungsvollen Position werden Sie als Qualitätssicherungsexperte tätig und tragen wesentlich zur Einhaltung regulatorischer Standards bei.\n\nIhre Aufgaben umfassen die Planung, Durchführung und Dokumentation von GCP- und GxP-Audits bei verschiedenen Partnern wie Investigator Sites, Clinical Research Organizations und Laboren. Sie erstellen risikobasierte Auditpläne, bewerten die regulatorische Compliance und steuern Qualitätsvorfälle inklusive CAPA- und Escalation-Management. Darüber hinaus entwickeln Sie das Qualitätsmanagementsystem weiter, unterstützen Clinical Operations als QA Business Partner und führen Lieferantenaudits durch. Sie bereiten Inspektionen vor und begleiten diese, während Sie gleichzeitig Schulungen zu GCP, GxP und qualitätsrelevanten Prozessen durchführen.\n\nFür diese Position bringen Sie ein abgeschlossenes Studium in Naturwissenschaften, Pharmazie oder Medizin mit. Sie verfügen über mindestens 10 Jahre Erfahrung in der klinischen Qualitätssicherung und mindestens 5 Jahre im Auditumfeld. Fundierte Kenntnisse in GCP (ICH-GCP E6), CTR, MDR und FDA-Regularien sind erforderlich. Nachweisbare Erfahrung in Auditierung und Inspektionsmanagement im klinischen Umfeld sowie im Umgang mit CAPA-Prozessen und Qualitätsmanagementsystemen runden Ihr Profil ab. Sehr gute Englischkenntnisse in Wort und Schrift sowie Bereitschaft zu nationalen und internationalen Dienstreisen werden vorausgesetzt.","de","FE55-07829-WIPL","https:\u002F\u002Ftouch.ferchau.com\u002Fde\u002Fde\u002Fprojekt\u002F496408",{"items":36},[37,57,73,89,108,126,141,157,172,189,198,210,227,241,257],{"id":38,"slug":39,"title":40,"skills":41,"budget":20,"duration":52,"location":53,"onsitePercent":22,"contractType":54,"foundAt":55,"category":56},10751,"global-clinical-order-manager","Global Clinical Order Manager",[42,43,44,45,46,11,47,48,49,50,51],"Clinical Supply Chain Management","SAP","GMP","Veeva","ERP systems","Master Data","German language","English language","Document management","Deviation management","12+ months, Start ASAP (01.08.2026)","Kaiseraugst","temp_work","2026-06-03T08:41:26+00:00",{"id":26,"slug":27,"label":28},{"id":58,"slug":59,"title":60,"skills":61,"budget":20,"duration":20,"location":69,"onsitePercent":22,"contractType":70,"foundAt":71,"category":72},7592,"initiativbewerbung-in-der-medizintechnik-mwd","Initiativbewerbung in der Medizintechnik (m\u002Fw\u002Fd)",[28,62,63,64,65,66,67,68],"Qualitätsmanagement","Technische Redaktion","Prozessmanagement","Projektmanagement","Englischkenntnisse","Flexibilität","Kommunikationsfähigkeiten","Kiel","permanent","2026-06-03T02:29:28+00:00",{"id":26,"slug":27,"label":28},{"id":74,"slug":75,"title":76,"skills":77,"budget":20,"duration":20,"location":85,"onsitePercent":86,"contractType":23,"foundAt":87,"category":88},7535,"biomarker-expert-clinical-biosample-operations-mwd","Biomarker Expert - Clinical Biosample Operations (m\u002Fw\u002Fd)",[9,78,79,80,81,82,83,84],"Kommunikationsfähigkeit","Koordination","Logistik","Optimierung","Organisationstalent","Probennahme","Prüfung","Biberach an der Riß",0,"2026-06-02T15:25:31+00:00",{"id":26,"slug":27,"label":28},{"id":90,"slug":91,"title":92,"skills":93,"budget":20,"duration":104,"location":105,"onsitePercent":20,"contractType":54,"foundAt":106,"category":107},7490,"technical-rd-analytical-project-lead","Technical R&D – Analytical Project Lead",[94,95,96,97,98,99,100,101,102,103],"HPLC","UHPLC","Mass Spectrometry","UV detection","Fluorescence","Analytical Chemistry","Chromatography","Project Management","Regulatory Documentation","English","12+ months","Basel","2026-06-02T13:06:41+00:00",{"id":26,"slug":27,"label":28},{"id":109,"slug":110,"title":111,"skills":112,"budget":20,"duration":122,"location":123,"onsitePercent":22,"contractType":23,"foundAt":124,"category":125},7364,"stellv-leitung-der-herstellung","Stellv. Leitung der Herstellung",[113,114,44,115,116,117,11,118,119,120,121],"Pharmatechnik","Biotechnologie","Aseptische Abfüllung","Batch Record Review","Change Controls","OEE-Systeme","Shopfloor-Management","Lean","OPEX","24 Monate (01.07.2026 - 30.06.2028)","Sachsen","2026-06-01T20:11:17+00:00",{"id":26,"slug":27,"label":28},{"id":127,"slug":128,"title":129,"skills":130,"budget":20,"duration":138,"location":105,"onsitePercent":20,"contractType":54,"foundAt":139,"category":140},7349,"rezept-und-methoden-spezialist","Rezept- und Methoden-Spezialist",[131,132,133,134,44,135,12,136,114,137,43],"Chemie- und Pharmatechnologie","PLS\u002FMES","PCS7","Unicorn Methodenrezeptierung","SOP","MSAT","Siemens","01.09.2026 bis 30.08.2027","2026-06-01T16:12:07+00:00",{"id":26,"slug":27,"label":28},{"id":142,"slug":143,"title":144,"skills":145,"budget":20,"duration":122,"location":153,"onsitePercent":154,"contractType":23,"foundAt":155,"category":156},7348,"stellvertretung-leitung-der-herstellung-amwhv","Stellvertretung Leitung der Herstellung (AMWHV)",[113,114,44,146,147,148,149,118,119,150,151,152,120,121,116,117,11],"Sterilabfüllung","aseptischer Bereich","Zytostatika","Drug Substance","AMWHV","AMG","US-FDA","Dessau-Roßlau",80,"2026-06-01T16:10:58+00:00",{"id":26,"slug":27,"label":28},{"id":158,"slug":159,"title":160,"skills":161,"budget":20,"duration":20,"location":169,"onsitePercent":22,"contractType":23,"foundAt":170,"category":171},7333,"packaging-labeling-spezialist-pharma-mwd","Packaging & Labeling Spezialist Pharma (m\u002Fw\u002Fd)",[162,163,44,164,165,166,167,168,65],"Biologie","Chemie","GDP","Pharmazie","Risikomanagement","MS Office","LIMS","Biberach","2026-06-01T15:26:29+00:00",{"id":26,"slug":27,"label":28},{"id":173,"slug":174,"title":175,"skills":176,"budget":20,"duration":20,"location":186,"onsitePercent":22,"contractType":23,"foundAt":187,"category":188},6439,"clinical-compliance-specialist-mwd-medical-devices","Clinical Compliance Specialist (m\u002Fw\u002Fd) Medical Devices",[177,178,14,179,180,181,182,183,184,185],"Clinical Evaluation","Medical Writing","ISO 14155","Post-Market Clinical Follow-up","Systematische Literaturrecherche","Medizinprodukte","Statistik","Zahnmedizin","Regulatorische Anforderungen","Bensheim","2026-05-28T07:25:35+00:00",{"id":26,"slug":27,"label":28},{"id":190,"slug":191,"title":192,"skills":193,"budget":20,"duration":20,"location":85,"onsitePercent":195,"contractType":23,"foundAt":196,"category":197},6425,"quality-specialist-pharma-mwd","Quality Specialist Pharma (m\u002Fw\u002Fd)",[44,62,165,114,163,166,8,194],"Teamfähigkeit",50,"2026-05-28T06:25:31+00:00",{"id":26,"slug":27,"label":28},{"id":199,"slug":200,"title":201,"skills":202,"budget":20,"duration":20,"location":207,"onsitePercent":195,"contractType":23,"foundAt":208,"category":209},6392,"qualitaetsmanager-mwd-medizintechnik","Qualitätsmanager (m\u002Fw\u002Fd) Medizintechnik",[62,28,203,8,167,204,205,206],"DIN 13485","Reklamationsmanagement","Validierung","Qualifizierung","Schwerin","2026-05-28T02:26:01+00:00",{"id":26,"slug":27,"label":28},{"id":211,"slug":212,"title":213,"skills":214,"budget":20,"duration":20,"location":224,"onsitePercent":195,"contractType":23,"foundAt":225,"category":226},6391,"experte-bildverarbeitung-medizintechnik-mwd","Experte Bildverarbeitung Medizintechnik (m\u002Fw\u002Fd)",[215,216,217,28,218,219,220,221,222,223],"Bildverarbeitung","C++","Python","Algorithmusentwicklung","Physik","Informatik","Sensoren","Bildfilterung","Rekonstruktion","Mannheim","2026-05-28T02:25:47+00:00",{"id":26,"slug":27,"label":28},{"id":228,"slug":229,"title":230,"skills":231,"budget":20,"duration":20,"location":85,"onsitePercent":22,"contractType":23,"foundAt":239,"category":240},6390,"technischer-assistent-mwd-wasseranalytik","Technischer Assistent (m\u002Fw\u002Fd) Wasseranalytik",[232,233,234,235,236,44,237,19,238,206,205],"Biologielaborant","BTA","MTA","mikrobiologische Testmethoden","Environmental Monitoring","Dateneingabe","Monitoring","2026-05-28T02:25:33+00:00",{"id":26,"slug":27,"label":28},{"id":242,"slug":243,"title":244,"skills":245,"budget":20,"duration":20,"location":254,"onsitePercent":195,"contractType":23,"foundAt":255,"category":256},6262,"softwareentwickler-c-medizintechnik-mwd","Softwareentwickler C++ Medizintechnik (m\u002Fw\u002Fd)",[216,246,247,248,249,250,251,28,252,253],"C#","C","CAN-Bus","Softwarearchitektur","Softwareentwicklung","Unit-Tests","Elektrotechnik","SCRUM","Jena","2026-05-27T11:28:50+00:00",{"id":26,"slug":27,"label":28},{"id":258,"slug":259,"title":260,"skills":261,"budget":20,"duration":104,"location":274,"onsitePercent":20,"contractType":54,"foundAt":275,"category":276},6245,"requirement-engineer","Requirement engineer",[262,263,264,265,266,267,268,269,270,271,272,273,103],"Requirements Engineering","ALM","CPRE\u002FIREB","CCBA\u002FIIBA","INCOSE","System Engineering","Software Engineering","Medical Engineering","IVD","V-model","EARS","German","Rotkreuz","2026-05-27T10:36:37+00:00",{"id":26,"slug":27,"label":28}]